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Variant (rsID / SNP)

rs542939

ABHD15

rs542939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABHD15. Location: chromosome 17, position 27,889,986. The table records no clinical significance for this variant.

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Reference-table entries

ABHD15Not classified
Variant type
missense_variant
Chromosome / position
17:27889986
HGVS
NM_198147.3,c.1000A>G,p.Thr334Ala
Allele change
Missense_T334A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.